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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407074Generated: October 29, 2026

Cesium carbonate → Methyl 3-{6-[(diphenylmethylene)amino]pyridazin-4-yl}benzoate

https://huagongshe.com/reaction/407074

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBenzophenone imineHCID 136809—
ReactantMethyl 3-(6-chloropyridazin-4-yl)benzoateHCID 86667186—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductMethyl 3-{6-[(diphenylmethylene)amino]pyridazin-4-yl}benzoateHCID 8666718569.6%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of methyl 3-(6-chloropyridazin-4-yl)benzoate (0.21 g, 0.84 mmol), benzophenone imine (260 μL, 1.5 mmol), (R)-(+)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (26 mg, 0.042 mmol), cesium carbonate (0.55 g, 1.7 mmol) and palladium acetate (9.5 mg, 0.042 mmol) in 1,4-dioxane (3 mL) was vacuum and refilled with nitrogen for 3 times. The reaction was stirred at 110° C. overnight. After cooling it was diluted with ethyl acetate. The organic solution was washed with water and brine, dried over Na2SO4. After filtration the filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in methylene chloride (0-20%) to afford the desired product (0.23 g). LCMS (M+H)+: m/z=394.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754114B2
Source datasetuspto-grants-2014_06
ORD IDord-bc17eb2769874d5aaed9652464303362
Source noteuspto-grants-2014_06